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rs1057524737

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524737(C;C)
Make rs1057524737(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166047622
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057524737
dbSNP (old)rs1057524737
ClinGenrs1057524737
ebirs1057524737
HLIrs1057524737
Exacrs1057524737
Gnomadrs1057524737
Varsomers1057524737
Maprs1057524737
PheGenIrs1057524737
Biobankrs1057524737
1000 genomesrs1057524737
hgdprs1057524737
ensemblrs1057524737
gopubmedrs1057524737
geneviewrs1057524737
scholarrs1057524737
googlers1057524737
pharmgkbrs1057524737
gwascentralrs1057524737
openSNPrs1057524737
23andMers1057524737
23andMe allrs1057524737
SNPshotrs1057524737
SNPdbers1057524737
MSV3drs1057524737
GWAS Ctlgrs1057524737
Max Magnitude0
ClinVar
Risk rs1057524737(C;C)
Alt rs1057524737(C;C)
Reference Rs1057524737(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904132C>G
CLNSRC
CLNACC RCV000443082.1,